Primary care symptoms and conditions

I had a kenalog shot a year and a half ago and over time my purple hole on my hip/but area was just getting bigger and bigger just last week my doctor cut it out it now is a nice straight line and all filled back in when she pulled the fat back together I am very happy with the results any primary care doctor should be able to do it and insurance should cover it because it is suspicious behaver of your skin. I am a medical assistant and this has really awakening and I make sure I use a appropriate needle every time and go nice and deep I would never want to scar one of my patients I think your nurse does not want to hurt you so she/he might use a shorter needle alot of us do not know about the divet/hole kenalog can cause I learned the hard way but I would rather the shot hurt a little and have no scar/divet.

I started NuvaRing 3 weeks ago yesterday after having the Mirena IUD removed (kept in all 5 years). I removed it yesterday as planned. 1 week ago, I felt a terrible pain in my right side under my ribs. I started having very slight trouble breathing, pain when laughing or coughing, etc. I applied heat and the pain subsided over the weekend and I could breathe easily. On Monday, I decided it best to go to the doctor since I had trouble breathing, I didn't want to assume it was nothing. I went to a doc in the box (bad idea) and I was told that I had a swollen rib cage (the cartilage). I'm certain I was misdiagnosed because the dude didn't even do xrays, even after I explained that I had just started NuvaRing. I wanted them to be aware of everything. The doctor dismissed it.

On Tuesday night, I was in so much pain and my difficulty breathing was worsening that I cried myself to sleep. Wednesday I went to work and was in so much pain that I was in tears and headed to URGENT Care, as my primary care physician could not fit me in. They xrayed, ran a urinalysis, a CBC to check my white blood cells and found nothing except for a bit of what appeared to be constipation, though I have regular bowel movements. My white blood count was slightly elevated, but distributed normally. I was prescribed a laxative and Lortab for the pain, which was excruciating. The doctor told me to come back the next day (today) to retest my white blood count. It went down a tad, as I had taken the Nuvaring out yesterday evening. The doctor seemed puzzled, but gave me my CBC results and urinalysis just in case I developed a fever or an infection of some sort, but told me that she thinks I am having side effects from the NuvaRing. She asked me to not put it back in.

On a side note, I had called my OBGYN on Wednesday before I headed to Urgent Care and explained the situation and they advised me to remove the NuvaRing as well.

I'll have to bite the bullet and pop the daily bc, such as Ortho Lo.

My daughter had switched from the birth control pill Low-Ogestrel-28 after about 2 1/2 years (no side effects at all then a little spotting mid cycle) so she saw her primary care and the dr. told her that her body had become used to that paticular pill and switched her to Yasmin. The first month was ok and then in the 2nd month I noticed a big change in her attitude..she became very short tempered during the entire month and then when she was on the placebo pills (the days prior to her period) she really became a crazy angry woman. When on the other bc the week prior found her more sensitive and crying...such a total flip in her nature.
Then on the 3rd month the vomiting began...nothing major at first - random maybe once a week and always in the morning...after juice or soymilk. So you explain it away by saying that it's first thing in the morning and theres more acid on your stomach or she was hungry when she went to bed and it's from that. She began having headaches around this time also..Ok so she stopped having anything but water with her English muffin first thing in the morning and things evened out with the stomach thing - for a little while. She was incredibly tired and had a weird sore throat - killer sore throat - never had strep before (she's 20 years old...) she got an appt. to see a N.P. in the dr. office and she asked me to go...while we were there I asked not only the medical assistant but the N.P. (nurse practitioner) about the law commercials that I had seen regarding Yasmin..they blew it off as just a bunch of ambulance chasers wanting money and that it was safe and effective. They were adamant about it. Ok I dropped it..after examination the NP told my daughter that her lymph nodes were enlarged and she had A. strep B. Mono C.all of the above. Tests ruled out Strep but we had a winner on Mono. While she had the week off from work I noticed depression along with the headaches and also the stomach problems came back. Always in the morning, but it became every morning now..we thought she was hungry and she would eat and feel fine and then about 5 minutes after finishing her breakfast with only a small amt. of water to go along with it she'd have a period where for the next 15 -30 minutes she'd either throw up (and once doing this would feel fine) or it would work itself out and she'd be fine. It had gotton to the point I don't know who dreaded the morning more her or me. We are now in the 4th month of Yasmin and this began to happen every single morning and then toward the end of the month it would start being random at nightime..no vomiting but feeling sick - like it had begun in the beginning with the morning stuff. It came to head the other day- Saturday October 10th 2009. We had gone on a overnight trip to see her grandparents and we had to leave early in the morning (4 am) so she took the pill after having a little something to eat (no liquids) by 2:30 that afternoon she all of a sudden felt like she was going to get sick..and boy did she - violently sick - then again at 6:30 - violently ill- projectile and again at 8:30. I got on the computer and started researching Yasmin....and it all came together. I told her no more pill...she is in a serious relationship and was using Yasmin not only for the terrible painful periods that she was having but for protection so we needed to take that into account...she was safe and she is now off that pill. She did not take one Sunday (11th) or Monday (12th) and I cannot tell you how much better she is. This was someone who had lived with a constant stomach ache for over 4 weeks...we could outfit a pharmacy with all the otc meds I have bought - pepto, rolaids, gaviscon, maalox, YOU Name it we have it in regards to stomach distress..and nothing really helped. A burp and feel better for a little while but it was always there..that low lying ache in the tummy. She spoke with a friend that works for a doctor on Sunday and told her about the Yasmin and the woman couldn't believe that she had been prescribed that..she told her to get off it immediately (she already had) and that the dr. that she works for will not prescribe Yasmin or yaz to any of his patients. My daughter's personality is back. She is laughing and happy and a totally different girl. Headaches are gone and most importantly NO stomach pain at all. Completely gone. She can eat and drink and no problems what-so-ever. She looked at me and said "I can't believe I lived like that for so long, I had forgotten what it felt like to feel good - like me". She is calling a Ob/Gyn practice this morning and hopefully will be seen by someone today. What a nightmare. My heart goes out to those of you that have posted and have had much worse things besides what my daughter has gone thru. The FDA needs to do something about this !! What can we do to get this information to them? DO NOT TAKE OR LET YOUR FAMILY MEMBERS TAKE YASMIN OR YAZ - IT IS HARMFUL.

I recently back in April of this year received Cyberknife radiation for Adenocarcinoma with metastasis to my brain. After surgery to remove my brain tumor in March of 2009. I went though whole brain radiation and the Cyberknife to my lung. The doctor was very adamant that as the lung heals from radiation you will develop what they call wet lung or neumonesis sp? This will have to be treated separately, or severe coughing would continue. My primary care doctor in the mean time put me on Lisinopril 20 mg for hypertension. I have not gotten a good nights sleep in 2.5 months since, then came the pneumonosis. This cough persist to this day waking me from what little sleep I do get, and amazingly am now suffering from joint pain especial in my hips. It's to the point I can't even cross my legs anymore it hurts. When discussing this with my primary she says its in my head as of today and reading this site and side effects I am taking myself off of Lisinopril and will seek a second opinion, even a third if need be thank you all so much for posting your side effects from this drug.

cannot believe how many stories I have read about mirena and hair loss etc..etc.. etc.. I have experienced many of the side effects that everyone is mentioning.. I actually feel I could live with most of them if it weren't for the hair loss. I have had ( copying from other post.. ridiculous right?)Tired all the time ~ Depression ~ Hungry all the time ~ leg cramps ~ HAIR LOSS TO THE POINT OF BALDING IN SEVERAL AREAS ~ oily skin and bad breakouts ~ Mood swings (huge...yelling fits at my husband and the kids) ~ fluttering in uterus~Sore breasts.. I have medium thick hair that is about 10 inches. I noticed a bald spot in June and now have discovered 4-5 others starting. I just had the iud removed today and my OB pretty much tried to convince me that there is no way that the IUD is causing my issues. I have never had any of these issues before. I got the Mirena on 4/30 of 08 and noticed slowly but surely all of the side effects mentioned. My OB told me that the progesterone could not be causing my issues because it is such a small dosage that it would be comparable to spitting in the ocean as far as the amount that is in my blood stream. She said because I am black and 35 that I may have an autoimmune disorder and that I should stop reading blogs. I told her that all of my research wasn't from a blog and that ALOPECIA is a side effect just not mentioned in my pamphlet that I can find. I understand what she is saying and that she is the one that is the dr. but nobody knows my body better than I do.. I am in it!! I have !never had any problems and have been healthy my entire life. There is no history of autoimmune disease in my family. I am going to my primary care doctor.. to have some blood tests done. I think that the mirena has caused an autoimmune response in my body.. it may not necessarily be the progesterone..although I don't rule it out no matter what she says . the progesterone is synthetic and has an androgynous like activity that is similar to testosterone the main thing that causes male pattern baldness. also Mirena is made out of Silicone.. perhaps those of us that are having hair loss are having it due to our body trying to fight off the foreign invader of the IUD itself. I was going to go and have the Paragard inserted.. because i was thinking it may just be the progesterone.. nope... I read that many women are complaining of ACNE and HAIRLOSS even with that because its made out of copper. So with that being said.. not sure what to do.. may have to go back on Yasmin.. didn't seem to have any problems with that.. I really just don't want to risk putting another hormone in my body.. We all need to get together and look into a class action suit because I am tired of being made to feel crazy by doctors.. sometimes what seems to not be possible is .. especially when there are so many women having the same problem. Feel free to e-mail me re: a class action suit.. if they took depo off Mirena needs to come of too. It seems like it has really screwed a lot of peoples system up.. Hopefully I won't find out I know have a thyroid problem etc.. etc..

cannot believe how many stories I have read about mirena and hair loss etc..etc.. etc.. I have experienced many of the side effects that everyone is mentioning.. I actually feel I could live with most of them if it weren't for the hair loss. I have had ( copying from other post.. ridiculous right?)Tired all the time
~ Depression
~ Hungry all the time
~ leg cramps
~ HAIR LOSS TO THE POINT OF BALDING IN SEVERAL AREAS
~ oily skin and bad breakouts
~ Mood swings (huge...yelling fits at my husband and the kids)
~ fluttering in uterus
~Sore breasts..

I have medium thick hair that is about 10 inches. I noticed a bald spot in June and now have discovered 4-5 others starting. I just had the iud removed today and my OB pretty much tried to convince me that there is no way that the IUD is causing my issues. I have never had any of these issues before. I got the Mirena on 4/30 of 08 and noticed slowly but surely all of the side effects mentioned. My OB told me that the progesterone could not be causing my issues because it is such a small dosage that it would be comparable to spitting in the ocean as far as the amount that is in my blood stream. She said because I am black and 35 that I may have an autoimmune disorder and that I should stop reading blogs. I told her that all of my research wasn't from a blog and that ALOPECIA is a side effect just not mentioned in my pamphlet that I can find. I understand what she is saying and that she is the one that is the doctor, but nobody knows my body better than I do.. I am in it!! I have never had any problems and have been healthy my entire life. There is no history of autoimmune disease in my family. I am going to my primary care doctor.. to have some blood tests done. I think that the mirena has caused an autoimmune response in my body.. it may not necessarily be the progesterone..although I don't rule it out no matter what she says . the progesterone is synthetic and has an androgynous like activity that is similar to testosterone the main thing that causes male pattern baldness. also Mirena is made out of Silicone.. perhaps those of us that are having hair loss are having it due to our body trying to fight off the foreign invader of the IUD itself. I was going to go and have the Paragard inserted.. because i was thinking it may just be the progesterone.. nope... I read that many women are complaining of ACNE and HAIRLOSS even with that because its made out of copper. So with that being said.. not sure what to do.. may have to go back on Yasmin.. didn't seem to have any problems with that.. I really just don't want to risk putting another hormone in my body.. We all need to get together and look into a class action suit because I am tired of being made to feel crazy by doctors.. sometimes what seems to not be possible is .. especially when there are so many women having the same problem. Feel free to e-mail me re: a class action suit.. if they took depo off Mirena needs to come of too. It seems like it has really screwed a lot of peoples system up.. Hopefully I won't find out I know have a thyroid problem etc.. etc.. ******e-mail me with Mirena in the subject line!!

I have been on omprazole 20mg 2x per day for 1 1/2 years. I went off of omeprazole in December of last year because I was tired of taking drugs. In February of this year I went to the ER because I thought I was having a heart attack (severe chest pain, pain shooting up my left jaw and my left arm was numb). The doctor in the ER gave me Mylanta with lidocaine and told me to go back on the omeprazole. I did and haven't missed a dose since that hospital visit. Until September 9, 2009 I took my regular dose of omeprazole (one in the morning and one in the evening) I was having a lot of discomfort and was uneasy. That day I also took two aspirins. I had continued stomach and chest discomfort and took some Mylanta. My old doctor had advised my to up my dose in severe situations and I took a third 20 mg dosage and within 10 minutes my face and arm went numb. I was rushed back to the hospital , my blood pressure was 144/81 and I was having panic attacks. I felt like I was going crazy. The doctor ordered bloodwork and a cat scan (because of the numbness) all came back normal. No one addressed the chest pain. Maybe because the EKG I had in February was normal (I don''t know). They had no answers and told me to follow-up with my primary care physician. I went home and finally tried to go to bed, I couldn't sleep well, my mind was racing. The next day the numbness and pins/needles went all over my body. Like everything just went to sleep. I tried to relax and stay calm. I finally went to bed that night but had a hard time falling to sleep (my mind was racing and I was scared). I eventually went to sleep and woke up with less numbness but I had a stiff and painful neck with a killer headache. I don't get headaches that often and this was a major concern for me. I called my insurance and they advised me to go in for an immediate care/same day appointment. I did which was also inconclusive but the doctor asked about my omeprazole. I told her I haven't taken any medications since I was seen at the hospital because I was scared it was something I took that caused the numbness. She didn't say that my symptoms were related to the omeprazole but told me to not take it again and only use Mylanta for my stomach problems. She was not a fan of this medication and told me it is over-prescribed. I have not taken the omperazole since September 9, 2009 and the numbness is almost gone but I still have the tingling and pins/needles from time-to-time and neck and chest pain. No headaches. The doctor gave me a mild muscle relaxer (for my neck pain) but with everything that has happened I haven't taken that either.
I have fibromyalgia and I manage my pain without medications and I do have random symptoms from time to time because of the fibromyalgia but these were acute and terrible. I have never experienced anything like this and I am hoping since I have stopped the omperazole I will go back to normal soon..........

I was taking prevacid for 6 years with no problems, then the insurance insisted I switch to omeprazole and after 2 weeks I developed severe upper abdominal pains, almost like a heart attack, with nausea, vomiting, weakness and cold sweats. It was a trip to the hospital and my primary care physician who swore that it could not be the Omeprazole and to continue. After the 2nd bout a week later I insisted that it was the meds and wanted something different. As I started taking something different I started feeling better after a couple of days and felt like I was over the problems after about 10 days and have had no problems since. Just the $7,000 medical bills.

Reading these is both disturbing and a relief. I was put on YASMIN by my GYN after blood work confirmed my estrogen was low- I was 42 at the time and the GYN felt I needed the pill to boost my energy and she said it would "even out" mood swings. I stayed on the pill for 3 years.

I attributed my fatigue to being "perimenaupasal" meanwhile I stopped the pill 3 weeks ago and my fatigue has lifted, my aches and pains are gone. When I would try to research these symptoms I would come up with Lupus or some chronic fatigue issue, but I realize now it was this pill making me fatigued, moody, and thirsty!!

I have had blood work done to rule out any other type of illness or issue and realize so many other women are struggling with these symptoms, the pill that is supposed to make life better is making people sick.

I have SEVERE leg pain, behind the knee, kneecap and just above my ankle, Also my hip. This is concentrated on my right side although I do have occasional pain on the left side. My primary care doctor said it was arthritis. When I told my GYN Dr. about this, her head snapped around very quickly. She said to stop the Fosamax and start on vitamin D, calcium and vitamin E. It has been 2 weeks, and the pain is still severe. I'd like to know when it will stop. Does anyone know?

Thank god I found this site! My body has been going crazy ever since I started taking Yasmin two years ago and I didn't put two and two together until reading all of these postings and realizing the Yasmin might be the culprit.

I'm a healthy 31 y.o. who exercises regularly, doesn't smoke and has been on various oral contraceptives for the last decade without too many side effects beyond slight moodiness and minor weight gain. About two years ago I switched over to Yasmin. About two months ago I came across this site as I was researching hypertension which I had developed. I was confused and didn’t know what was causing it as I am healthy, unstressed and have a history of low blood pressure. But as soon as I found this site it all started coming together and I realized Yasmin had done much more than raise my blood pressure. I immediately went off the pill and almost right away many of my side effects went away. Here's what I've experienced since being on the pill:

-Weight Gain: Almost right away I gained ten pounds. I’ve effortlessly lost five of those pounds since going off the pill.
-Seborrheic Dermatitis: After a few months of being on Yasmin I developed a painful scalp condition called Seborrheic Dermatitis. Side effects of this are inflamed scalp, redness and most importantly, hair loss. The doctor said it is generally brought on by stress but on further research I saw that it is also caused by hormones, so it wasn’t a stretch for me to realize Yasmin might be the culprit once I saw this site. Over the last couple years I’ve been using all sorts of prescription shampoos to make the problem go away and nothing helped. But as soon as I went off the pill my scalp condition cleared in only a month without the use of shampoos.
-High Blood Pressure: Before I went on the pill my BP was about 100/70. During the time I took Yasmin my BP slowly climbed to above 140/90. Within two weeks of going off the pill my BP was back down to pre-Yasmin levels.
-Irregular Heart Beat: After about a year and a half of being on the pill I started to suffer from seriously irregular heart beat which went away immediately after I got off Yasmin.
-Hyperpigmentation: I know any birth control can cause this but none of them ever have until I went on Yasmin at which point it sprung up all over my face. I’m hoping the dermatologist can clear it up now that I’m off the pill.
-Tightness in Chest: Happened around same time as irregular heartbeat and is now gone.
-Anxiety: I’m not sure I can blame Yasmin for this one since going off Yasmin has not caused it to go away. But enough posters on this site mentioned it as a side effect and it wasn’t a problem for me pre-Yasmin, so I wanted to mention it.
-Irritability: I’m generally easy going and don’t let the little things bother me, but as soon as I went on Yasmin everything started to bug me. Now that I’m off Yasmin I’ve been in a much better mood.

If anyone is on this pill or thinking about going on it, I implore you not to. Too many risks especially since there are so many other pills out there that don’t have many side effects. I mean, there are close to 5,000 postings on this site, mostly against this pill while if you search the web there are almost no other pills that generate this kind of attention. That alone tells me something. I hope the makers of the pill pull it from the market immediately or doctors stop recommending it.

My son has been taking Keppra since his first seizure last year when he was 18, starting out with 500g. He kept having the seizures (all grand mal) off and on and because he was planning on going into the military, he was told that because of the seizure disorder, he could not serve. Given a medical discharge and coming home, he still had them, but the cause was because at times he forgot to take his meds or he worked out over exerting himself, stuff like that. From the end of April until July 6th, he did not have a seizure (his Keppra was increased to 3000g a day), and that seizure was not as bad as the previous ones he had.

We ended up switching doctors because the original doc did not want to do an eeg on my son, so with my husband and my decision plus our primary care physician agreeing, we starting having my son see a new doc. This doc seems to really care about his patients, and after talking with us, he gave my son a prescription for Depakote, 500mg three times a day along with the Keppra. A day and a half after taking the drug (the first day he took it at night then taking it as prescribed daily), he started vomiting. He would eat, later on lay down, wake up EXTREMELY nauseous, and start throwing up. This happened for four and a half days, and the doctor told him to stop taking the meds immediately. He did blood work again and said that his Depakote serum levels had dropped drastically and he wanted to put my son back on the Depakote, but at half strength; 250mg three times a day. Our answer to that? HELL NO!!! My son was miserable; he has a job and hangs out with his friends and not being sure if he would start throwing up again, he minimized going out except to go to work. It is frustrating as all HELL, took that crap for six days and four and a half of those days he was vomiting, unsteady on his feet, eyes were red looking like he was a zombie, and had starting messing with his memory in ONLY SIX DAYS! Yes we all want him to be free from this demon, and so far for these past few months of this year, (from end of April to July 6) he has had one seizure. He has not had another one since that day. As far as we are concerned as his parents, he will never take that crap again, I don't care WHAT this doctor says. And I am going to say that I believe that my son will not want to take it again either, even at a lower dose.

I took the time to call the company who manufactures the Depakote, and one of the reps I spoke to said that even if my son took a lower dose, it could still have the effects of vomiting as with the higher dose, and her concern is that when he is throwing up, he is also throwing up the Keppra which could cause him to have a seizure. NOBODY wants that!

I had Mirena put in on July 2nd. I had it removed today (August 4th). I gained 10lbs in 3 weeks, my hair is falling out like crazy, my face is breaking out, I was having kidney pain and the most recent was on Sunday when I couldn't get out of bed due to severe back pain and I couldn't lift my right leg. My husband had to pull me out of bed so I could use the bathroom. Any time I sat down, he had to pull me up. As the day went on, I could slowly start moving more. Yesterday and today my back was still very tender. I had it removed @ 3:30 this afternoon and my back pain and tenderness is completely gone (it's now 8:15 p.m.) My doctor told me that Progesterone is what causes all of those symptoms so he recommended I wait 2-3 months before trying any kind of birth control to get all of the hormones out of my body and make sure it's not a thyroid issue. Two people I know have Mirena and they have no symptoms and they love it. I on the other hand, can't say the same. I think people sensitive to progesterone need to find a different route.

I received my 1st gardasil 2 weeks ago. Right after receiving it, i felt very dizzy. I layed in the hospital for 30 minutes before i felt any better. The next day my right elbow started hurting, a couple days later my left elbow. My chest started hurting and it felt very heavy to breathe. My heart beats very rapid at times and makes me feel light headed. My arms feel tingly/numb at times, so i called my doctor yesterday to report this, she said these symptoms had nothing to do with gardasil and i needed to see my primary care physician. I would not advise anyone to get this shot. I will not go back to receive the other 2 shots.

After taking Chantix for one month I now have breathing problems. I took
Chantix in November 2007. My last day of smoking was November 22,2007
I Started having breathing problems in late December 2007.

Hello! I am 26 and a mother of 3 boys. I had C sections with all of them so since I didn't dilate insertion of Mirena was quite painful. I had it inserted 9/29/2008. The first few months were not bad. Had a period like every other month and spotted the ones in between. Starting in April-May I was having labor type pains so I called her, she checked it and I had an ultrasound, all LOOKED good. Well here I am 06/17/2009 and I have just made an appointment for removal! I feel like crap. I'm excessively bitchy, and I feel preggo! Bloated, crampy, and fatigued. I'm just tired of it. The nurse had told me I continue to have issues I can get it removed and then if I still have issues to go to my Primary Care Doctor. I know its the Mirena. I will just have to prove it when I have it taken out and I see her again for my yearly in Sept. The doctor is so sweet but the nurse makes me feel like I'm just complaining. I just hope I return to normal after.

Can anyone email me who has had it taken out and tell me how you feel after?
******

Thanks!

Just want to survey everyone and ask for responses for the following 3 questions:

1. how long did you keep your Mirena and if you no longer have it, why did you have it removed?

2. how many of you had your thyroid checked? who's came back abnormal? what were the levels?

(I'm a medical student doing research on this one since I believe the levonorgestrel affects our thyroid hormone. My TSH was elevated to 5.2 which is considered "subclinical HYPOthyroidism". This was mid cycle when my natural progesterone AND synthetic progestin were cumulatively high. When I had it rechecked 6 weeks later (around my period when any natural progesterone level is gone) it was normalized at 1.5. So I think that the P+P screws up our thyroid and can throw us into a high TSH and "hypothyroid state". The opposite effect may be true during menstruation and we can become HYPERthyroid for a few days... hence the really bad anxiety?!)

3. where is everyone from? perhaps we can have support group meetings?

I am 40 years old and recently went to my medical facility as I have had a "viral" ear infection for almost a year now, and it is concerning me. I do not take medication typically. My new primary care provider recommended I try Singulair. So far I have taken three doses over three nights. The first night was horrifying, the dreams I had were so scary, and they were tied into reality which was even stranger as the drug also makes you wake up often, then when you fall back asleep your awake time ties into your dreams. I woke up in a numb state. Since then, I also have been extremely agitated, dizzy, mouth sores, acne, fuzzy thinking, light headed and severe fatigue and body aches. Thank goodness I checked out this webpage, as I too will stop taking this drug. I find it very disappointing, how are we suppose to be able to trust our medical professionals to help us with one of our most prized possessions, our bodies, when we are given something to clear up an ear infection only to have it affect numerous other aspects of our lives to such a serious degree with no mention from our medical professionals. This is ridiculous. I guess I'll live with the viral ear infection.......

I am posting this because I feel so strongly about warning young ladies of the side effects of mirena. I am a mom with 3 small children and wanted an easy birth control. I had the mirena for 2 1/2 years. The first few months were okay but then I started to notice no sex drive, I slowly gained 15-20 pounds even exercise and diet change would not slow down, and i was very irritable. My poor family! I also started having what my primary care doctor diagnosed as anxiety attacks. I didn't even know what one was until I began to have them. I would get a hot flash, my heart would start pounding and I would start breathing fast. I felt like I would pass out and I had no idea where it was coming from. I had to get up and walk out of appointments, and even church. I then googled mirena side effects to find many others had the same experience. My doctor told me he didn't think my symptoms were related to the mirena. I know myself and I know when something is wrong.
I had it removed 3 months ago and I am only now more convinced the feelings I was having were caused by mirena. Slowly, I can feel my body return to normal and have lost 5 pounds. I hope this blog is helpful.
If you are having life altering side effects like I did, insist that your doctor remove it. Birth control does not have to be at the cost of your sanity!!

I was taking Topamax for about 4 years for chronic/daily migraines. It helped tremendously after I had taken almost everything else with no success. Then I had an episode where I ended up with 5 kidney stones. They passed but my neurologist wanted me off the Topamax in case that was the cause of them. I went off and my headaches came back with a vengeance. I had them daily until I begged my primary care doctor to put me back on Topamax. I honestly would rather have stones than daily headaches. I am a mother to four and have a husband and a job. I can't live with daily migraines. After being back on it for about two weeks the headaches have disappeared. I take 200 mg twice a day. I do have memory loss and loss of words big time. It is VERY frustrating. I feel stupid. But I can live with that. I have tingling cheeks , lips and hands. I'm sensitive to sun and have to wear my sunglasses a lot more now. I now talk in my sleep- a little nervous about that :) I lost weight last time around but haven't yet this time. I am very happy, not sure if that is the RX or just me reacting to not having headaches. I guess you have to weight the side effects with the benefits. The choice is ultimately up to you. Good luck everyone!

Unfortunately I've had to stop the Lupron injections. I lost my job and with that my health insurance. I am wondering can anyone tell me when I can expect my period to start again?

November 6, 2008 was my last injection and it was a 3 month dose. It is May 2009, I am 39 years old and I have not yet had a period. My fibroids ae back to their large abdomen filling size so I am very worried.

Not having insurance or adequate funds has reduced me to the internet for research first before venturing out to a doctor as a "self-pay" patient.

I have been on lisiniprol with hctz on 10mg dose since October 2008. My BP averaged around 144/95 before taking the med, now averages about 122/78. The problem i am having is this constant "tickle" in my throat which has been giving me coughing fits. When i breathe in deep i can feel a sensation to cough, sometimes my throat feels tight and sore, the first time i felt this was December 2008 and the doctor said it was a touch of post nasal drip and this was before i have read stuff on this board. Has anyone else experienced this kind of sensation in the throat? sometimes when i talk i even have to cough, i experimented once and did not take my dose and it seemed my throat felt better but then noticed my bp went right back up, i guess i better tell the doctor to get me off of this drug. She did tell me that the cough was part of the side effect. thanks and hope someone answers this.

I had been taking this for years and about three-four yrs ago they changed generic. I had horrible stomach and abdominal problems.Not diarrhea or constipation but pain swelling bloating and feeling a lump in ab. Went to cts, ultrasounds, 3 colonoscopies,endoscopy, pill camera,I went through 3 primary care doctors. Had emergency hosp.visits. Doctors.started getting to think I was crazy That made me depressed to the point I didn"t want to see anyone or go any where. Not one Dr. suggested it could be one of my meds. By accident over the Christmas holidays I ran out of my lisinopril hctz. within 3 days I felt normal again Swelling in ab stopped and most of pain.ever gonna get near that poison again.# months later Im doing a lot better I actually feel good .Its amazing I think it caused me a rare reaction called intestinal angioedema .That is basically hives on your insides. Could be dangerous if esophogeous is involved I lucked out.I did have wheezing and shortness in breathing .People Beware Its a dangerous drug.

I had the mirena placed about 2 months ago, a year after my daughter was born. i was ready to start dating again and i figured this was a safe second protection for me. 2-3 weeks later i had a yeast infection, i've never had a yeast infection in my life, i'm 29yrs old. I was so scared i thought i had an STD. I scheduled an apt ASAP with my primary care Dr. yes it was a yeast infection but i did not think it was the mirena. After that my "girl" hasn't been the same. ive had this slight burning sensation all the time. my "girl" is swollen and irritated and i now have another yeast infection. I became concerned and started to research yeast infection and came across this site and instantly I knew what was wrong. i'm getting this thing out my body instantly. I'm also hypothyroid because of thyroidectomy surgery and thought my new symptoms were because my synthroid doses were being adjusted once again but now it seems the mirena is also to blame. Either way i'm getting the mirena out because of the yeast infection alone. this is making me crazy.